The ubiquitin proteasome system in neurodegenerative diseases: Culprit, accomplice or victim?

被引:101
作者
Dennissen, F. J. A. [1 ]
Kholod, N. [1 ]
van Leeuwen, F. W. [1 ]
机构
[1] Maastricht Univ, Fac Hlth Med & Life Sci, Dept Neurosci, NL-6200 MD Maastricht, Netherlands
关键词
Neurodegenerative diseases; Ubiquitin proteasome system; Alzheimer's disease; Parkinson's disease; Huntington's disease; Frontotemporal dementia; Amyotrophic lateral sclerosis; Ubiquitin; Protein degradation; Ubiquitin-like proteins; AMYOTROPHIC-LATERAL-SCLEROSIS; FRONTOTEMPORAL LOBAR DEGENERATION; DEPENDENT PROTEOLYTIC SYSTEM; CU/ZN SUPEROXIDE-DISMUTASE; AMYLOID PRECURSOR PROTEIN; CONJUGATING ENZYME E2-25K; ALPHA-SYNUCLEIN; PARKINSONS-DISEASE; HUNTINGTONS-DISEASE; MUTANT UBIQUITIN;
D O I
10.1016/j.pneurobio.2012.01.003
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
A shared hallmark for many neurodegenerative disorders is the accumulation of toxic protein species which is assumed to be the cause for these diseases. Since the ubiquitin proteasome system (UPS) is the most important pathway for selective protein degradation it is likely that it is involved in the aetiology neurodegenerative disorders. Indeed, impairment of the UPS has been reported to occur during neurodegeneration. Although accumulation of toxic protein species (amyloid beta) are in turn known to impair the UPS the relationship is not necessarily causal. We provide an overview of the most recent insights in the roles the UPS plays in protein degradation and other processes. Additionally, we discuss the role of the UPS in clearance of the toxic proteins known to accumulate in the hallmarks of neurodegenerative diseases. The present paper will focus on critically reviewing the involvement of the UPS in specific neurodegenerative diseases and will discuss if UPS impairment is a cause, a consequence or both of the disease. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:190 / 207
页数:18
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